Both estrogen receptor α and estrogen receptor β agonists enhance cell proliferation in the dentate gyrus of adult female rats

Neuroscience ◽  
2006 ◽  
Vol 141 (4) ◽  
pp. 1793-1800 ◽  
Author(s):  
C.A. Mazzucco ◽  
S.E. Lieblich ◽  
B.I. Bingham ◽  
M.A. Williamson ◽  
V. Viau ◽  
...  
2005 ◽  
Vol 66 (2) ◽  
pp. 142-149 ◽  
Author(s):  
Anna I. Nagy ◽  
Brandi K. Ormerod ◽  
Christine Mazzucco ◽  
Liisa A.M. Galea

2001 ◽  
Vol 91 (5) ◽  
pp. 2400-2406 ◽  
Author(s):  
Ram V. Sharma ◽  
Milind V. Gurjar ◽  
Ramesh C. Bhalla

Epidemiological studies have demonstrated that hormone replacement therapy with estrogen (E2) or E2plus progesterone in postmenopausal women decreases the age-associated risk of cardiovascular disease by 30–50%. Treatment of vascular smooth muscle (VSM) cells with physiological concentrations of E2 has been shown to inhibit growth factor-stimulated cell proliferation. In this study, we tested the hypothesis that E2 inhibits the age-associated increase in VSM cell proliferation by inhibiting nuclear factor (NF)-κB pathway. We investigated the effects of E2 treatment and adenovirus-mediated estrogen receptor (ER)-α gene transfer on cell proliferation and NF-κB activation using VSM cells cultured from 3-mo-old and 24-mo-old Fischer 344 female rats. Our results demonstrate that VSM cell proliferation was significantly increased ( P < 0.05) in aged compared with young adult female rats. Treatment of VSM cells with physiological concentrations of E2 inhibited VSM cell proliferation, and this inhibition was significantly greater ( P < 0.05) in cells from aged female rats compared with young adults. The inhibitory effects of E2 on cell proliferation in aged female rats were significantly potentiated by overexpression of the human ER-α gene into VSM cells. Constitutive and interleukin (IL)-1β-stimulated NF-κB activation was significantly greater ( P < 0.05) in VSM cells from aged compared with young female rats. E2 treatment of VSM cells from aged female rats inhibited both constitutive and IL-1β-stimulated NF-κB activation. ER-α gene transfer into VSM cells from aged female rats further augmented the inhibitory effects of E2. In conclusion, our data demonstrate that constitutive and IL-1β-stimulated NF-κB activation is increased in VSM cells from aged female rats due to loss of E2 and this can be restored back to normal levels by ER-α gene transfer and E2 treatment. In addition, increased NF-κB signaling may be responsible for increased incidence of cardiovascular disease in postmenopausal females.


2004 ◽  
Vol 171 (4S) ◽  
pp. 348-348
Author(s):  
Ellen Shapiro ◽  
Hongying Huang ◽  
Rachael R. Mash ◽  
Eliza Ng ◽  
Deborah E. McFadden ◽  
...  

1997 ◽  
Vol 11 (10) ◽  
pp. 1486-1496 ◽  
Author(s):  
Katarina Pettersson ◽  
Kaj Grandien ◽  
George G. J. M. Kuiper ◽  
Jan-Åke Gustafsson

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